rs1736135
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1736135(C;C) |
| Make rs1736135(C;T) |
| Make rs1736135(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 15432901 |
| Gene | LOC101927745 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1736135 |
| dbSNP (classic) | rs1736135 |
| ClinGen | rs1736135 |
| ebi | rs1736135 |
| HLI | rs1736135 |
| Exac | rs1736135 |
| Gnomad | rs1736135 |
| Varsome | rs1736135 |
| LitVar | rs1736135 |
| Map | rs1736135 |
| PheGenI | rs1736135 |
| Biobank | rs1736135 |
| 1000 genomes | rs1736135 |
| hgdp | rs1736135 |
| ensembl | rs1736135 |
| geneview | rs1736135 |
| scholar | rs1736135 |
| rs1736135 | |
| pharmgkb | rs1736135 |
| gwascentral | rs1736135 |
| openSNP | rs1736135 |
| 23andMe | rs1736135 |
| SNPshot | rs1736135 |
| SNPdbe | rs1736135 |
| MSV3d | rs1736135 |
| GWAS Ctlg | rs1736135 |
| GMAF | 0.2718 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18587394 ]
|
| Trait | Crohn's disease |
| Title | Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease |
| Risk Allele | T |
| P-val | 6.9999999999999998E-9 |
| Odds Ratio | 1.18 [NR] |
| GWAS snp | |
|---|---|
| PMID | [PMID 20228799]
|
| Trait | Ulcerative colitis |
| Title | Genome-wide association identifies multiple ulcerative colitis susceptibility loci |
| Risk Allele | T |
| P-val | 2E-7 |
| Odds Ratio | 1.20 [NR] |
[PMID 19068216] Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.
[PMID 21304977] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
